Enchenopa chocoandina, Rueda-Rodríguez & Montalvo-Salazar, 2024
publication ID |
https://doi.org/ 10.3897/zookeys.1216.124181 |
publication LSID |
lsid:zoobank.org:pub:4258382E-C1BE-4969-8240-C1251459D2DD |
DOI |
https://doi.org/10.5281/zenodo.13962595 |
persistent identifier |
https://treatment.plazi.org/id/91C5558F-607B-5F62-9E5C-D8719E55B6AB |
treatment provided by |
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scientific name |
Enchenopa chocoandina |
status |
sp. nov. |
Enchenopa chocoandina sp. nov.
Figs 5 View Figure 5 , 6 View Figure 6 , 7 View Figure 7 , 8 View Figure 8
Material examined.
Holotype: Ecuador • 1 ♂; Pichincha, Tandayapa Cloud Forest Station -0.009645, -78.688058, 2280 m of elevation; 3 Fbr. 2024; Rueda, M. P. leg.; Ex. Manual; ZSFQ -i18060 GoogleMaps . Paratypes: Ecuador • 1 ♂; same data as for holotype; ZSFQ -i18061 GoogleMaps • 3 ♀, 1 ♂; Pichincha, Tandayapa Cloud Forest Station -0.009645, -78.688058, 2280 m of elevation; 9 Fbr. 2024; López-García, M. M., Montalvo, J. & Rueda, M. P. leg.; Ex. Mercury light; ZSFQ -i10862 : 10865 GoogleMaps • 1 ♀; Pichincha, Mindo , 0.04166, -78.77472, 1300 m of elevation; 11 Jun. 2022; Torres, D. leg.; Ex. Manual; ZSFQ -i8423 GoogleMaps • 1 ♀, Imbabura, Seis de Julio de Cuellaje , 0.4509352, -78.525948, 2000 m of elevation; 13 Nov. 2021; Rubio, A. leg.; Ex. Manual; ZSFQ -i8196 GoogleMaps .
Note on the type series.
Holotype and most paratypes are minuten-mounted. The paratype female ZSFQ -i8243 was originally pinned, but later the specimen was transferred to double mounting on a minuten pin. Dissected abdomens of holotype, one male paratype, and three female specimens placed in vials with glycerol pinned with specimens.
Diagnosis.
Overall coloration black with scarlet median carina and posterior apex in females and scarlet posterior apex in males, apical 1 / 3 of forewing amber; pronotal horn absent, replaced by obtuse projection directed obliquely forwards, lateral carina almost touching lateral margin of pronotum; three or four weak accessory carinae, some touching lateral carinae or bifurcate.
Description.
Male holotype ( ZSFQ -i10860 ): Measurements (mm): Length from head to wings: 5.3; Total length: 5.4; Head to apex of posterior process: 4.5; Pronotal length: 4.6; Head to horn apex: 1.5; Forewing length: 4.4; Body width: 2.2; Vertex width on ocellar line: 1.2; Head length: 1.2; Frontoclypeus length: 0.7; Frontoclypeus width: 0.1; Metathoracic tibia length: 0.9; Prothoracic tibia length: 1.8; Metathoracic tibia width: 0.3; Prothoracic tibia width: 0.2.
Color. Overall color black. Eyes brownish, ocelli golden. Posterior apex of pronotum scarlet red. Forewings almost entirely opaque black with an apical translucent amber patch restricted on the third to fifth apical cells and limbus around this area. Tarsi pale brownish.
Surface. Head, pronotum, ventral sclerites of thorax, legs, and abdomen with golden pubescence (Fig. 5 B View Figure 5 ); sclerotized area of forewings with shorter pubescence. Pronotum (except by metopidium) and sclerotized area of forewings strongly punctured. Head, metopidium, legs, and abdomen rough.
Head. Triangular blunt, longer than wide (excluding eyes); distance between ocelli subequal to ocelli-eye distance; supra-antennal ledges arranged above clypeus; clypeus broad, longer than wide, anterior margin rounded; rostrum reaching posterior coxae (Fig. 5 A View Figure 5 ).
Thorax. Pronotum, in lateral view, triangular; metopidium straight directed forwards; pronotal horn absent instead an obtuse projection with rounded apex; humeral angles slightly produced (Fig. 5 B View Figure 5 ); median carina sharp; lateral carina parallel to median carina, running from apex of anterior projection to middle of the lateral margin of pronotum, almost touching the margin (Fig. 5 C View Figure 5 ); three accessory carinae short (1 / 10 length of lateral carina), weak, irregular, sub-perpendicular to primary lateral carina, the last two diverging from the lateral carina (Fig. 5 D View Figure 5 ), left side with the anterior two accessory carinae convergent; posterior apex of pronotum acuminate, just surpassing first apical cell. Forewing with one vein on clavus, two discoidal cells, two m-cu cross veins, one s cross veins which enclose second discoidal cell, and five apical cells; apical limbus broad. Anterior and middle tibiae foliaceous; posterior femur with apical ventral and middle cucullate setae, posterior tibia with spine-like cucullate setae on rows I and II, row III absent.
Abdomen. Sternum III with a transversal keel extended along the sternite, strongly projected downwards and medially invaginated. Tergites III to VI with a pair of medial tuberosities, tuberosities of tergite VI strongly developed (Fig. 6 D View Figure 6 ). Subgenital plate, in lateral view, 3 × longer than wide, lobes diverging since the base, dorsal margin concave (Fig. 6 A View Figure 6 ). Aedeagus with posterior arm lanceolate, 2 × longer than anterior arm and strongly inclined forwards; anterior face of posterior arm armed at apical 1 / 3 with small dorsal apical denticles, gonopore subapically (Fig. 6 C View Figure 6 ). Styles distally recurved, apically truncate with anterior part longer than posterior part, spine tuft on dorsal margin just anterior to apex (Fig. 6 B View Figure 6 ).
Female paratype ( ZSFQ -i8423 ): Similar to male except for the pronotal projection more angulated and produced, central carina reddish behind humeral angles and forewings with amber patch extended from the second to fifth apical cells and limbus around this area. Genitalia. Gonoplac ventrally setose and more sclerotized than dorsally (Fig. 6 E View Figure 6 ). First valvula blade shaped, basal 2 / 3 broad, apex acuminate (Fig. 6 F View Figure 6 ). Second valvulae blade shaped with two dorsal tubercles in apical 1 / 2 (Fig. 6 G, H View Figure 6 ).
Nymph unknown.
Variation.
Measurements. Female / male (mm): Length from head to wings: 5.7–5.9 / 5.3–5.5; Total length: 5.9–6.4 / 5.4–5.7; Head to apex of posterior process: 5–5.6 / 4.3–4.5; Pronotal length: 4.9–5.5 / 4.5–4.6; Head to horn apex: 1.6–1.9 / 1.5–1.8; Forewing length: 5–5.4 / 4.4–4.8; Body width: 2.3–2.7 / 2.1–2.2; Vertex width on ocellar line: 1.2–1.4 / 1.1–1.2; Head length: 1.3–1.5 / 1.0–1.2; Frontoclypeus length: 0.7–0.9 / 0.7–0.8; Frontoclypeus width: 0.8–1.0 / 0.7–0.9; Metathoracic tibia length: 1–1.2 / 0.9–1.1; Prothoracic tibial length: 1.5–1.9 / 1.8–1.9; Metathoracic tibia width: 0.3–0.4 / 0.3–0.3; Prothoracic tibia width: 0.2–0.4 / 0.2–0.3.
Females are longer and have more produced pronotal projections than males (Fig. 7 A, C View Figure 7 ), three or four accessory carinae (Fig. 7 D View Figure 7 ), lateral carina behind humeral angles reddish rather than just the posterior apex of pronotum, and the amber membrane is most extended (Fig. 7 B View Figure 7 ). Independent of gender, some accessory carinae are bifurcate or converged.
Distribution and natural history.
This species is distributed in the Montane forests of northwest Ecuadorian Andes (Fig. 9 View Figure 9 ), between 1300 to 2300 m elevation. It inhabits the borders of secondary forests (Fig. 8 B View Figure 8 ) and is a solitary species. The species has been recorded perched on the leaves or stems of different species of Asteraceae and Araceae , but more oftenly on Munnozia pinnatipartita (Hieron.) H. Rob. & Brettell ( Asteraceae ) (Fig. 8 A View Figure 8 ), an endemic Ecuadorian species ( Barriga et al. 2011). The species has been observed active during the day and attracted to mercury light traps at night between 8 pm and 2 am (Fig. 8 C View Figure 8 ).
Etymology.
The species, a noun in apposition, is named after the Andean Choco Biosphere Reserve declared by UNESCO as the seventh biosphere reserve of Ecuador, where this species lives. It honors the people who defend this territory from the metal mining that threatens the ecosystems and biodiversity of this important area.
Remarks.
Enchenopa chocoandina sp. nov. belongs to E. andina species group based on the pronotum with a horn or projection shorter than the distance between the humeral angles, the forewing with transparent patches, and the blade-shaped second valvulae. Moreover, some species of this group, such as E. pilosa and E. eurycephala , have dense pubescence, shared with E. chocoandina sp. nov.
Enchenopa chocoandina sp. nov. differs from Enchenopa loranthacina ( Sakakibara & Marques, 2010) by the obtuse projection obliquely directed forwards rather than a horizontally inclined horn and from E. pilosa Strümpel & Strümpel, 2014 and E. eurycephala Strümpel & Strümpel, 2014 by the head longer than wide instead of as long as wide or wider than long respectively. Enchenopa chocoandina sp. nov. has a reddish median pronotal carina and amber forewing patches which separate it from E. monoceros ( Germar, 1821) and E. luizae ( Lencioni-Neto & Sakakibara, 2015) which have the median carina concolorous and forewing patches hyaline. The new species resembles E. andina ( Schmidt, 1924) by the black overall coloration with median carina and posterior apex reddish, and the amber forewing apex; however, E. chocoandina sp. nov. does not have a horn instead an obtuse projection, longer and denser pubescence, and three or four weak and irregular accessory carinae instead of two or three. Moreover, the new species is considerably shorter than E. andina and differs in the male and female genitalia.
Enchenopa chocoandina sp. nov. lacks a distinctive horn; instead, it has an obtuse projection with a rounded apex, resembling species of the E. beebi species group or the males of E. minuta species group ( Strümpel and Strümpel 2014). However, E. chocoandina sp. nov. properly does not fit within the E. beebi species group due to the absence of large punctation on the upper portion of the pronotum and dorsum, a short translucent apical patch and yellow tarsi. Neither does it belong to the E. minuta species group due to the absence of sexual dimorphism in pronotal horn shape; in E. chocoandina both females and males lack a horn.
We suggest E. andina and E. chocoandina sp. nov. could be related species by the scarlet median carina and posterior apex only shared in both species. Both inhabit mountain forests of the north Andes of Ecuador however are geographically separated by the Interandean Valley.
No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.
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